ClearanceBrief
510(k) K090408 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO: DSS STABILIZATION SYSTEM

ApplicantParadigm Spine, LLC, Washington DC, US
DecisionUnknown, Mar 20, 2009
ReceivedFeb 18, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K090408

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.